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WHO Drug Information Vol. 18, No. 2, 2004 - World Health ...

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Proposed INN: List 91 <strong>WHO</strong> <strong>Drug</strong> <strong>Information</strong>, <strong>Vol</strong>. <strong>18</strong>, <strong>No</strong>. 2, <strong>2004</strong><br />

palosuranum<br />

palosuran 1-[2-(4-benzyl-4-hydroxypiperidin-1-yl)ethyl]-3-(2-methylquinolin-<br />

4-yl)urea<br />

urotensin receptor antagonist<br />

176<br />

palosuran 1-[2-(4-benzyl-4-hydroxypipéridin-1-yl)éthyl]-3-(2-méthylquinoléin-<br />

4-yl)urée<br />

antagoniste du récepteur de l'urotensine<br />

palosurán 1-[2-(4-bencil-4-hidroxipiperidin-1-il)etil]-3-(2-metilquinolin-4-il)urea<br />

antagonista del receptor de la urotensina<br />

C25H30N4O2<br />

N<br />

CH 3<br />

N<br />

H<br />

O<br />

N<br />

H<br />

N<br />

OH<br />

540769-28-6<br />

panitumumabum<br />

panitumumab immunoglobulin, anti-(human epidermal growth factor receptor)<br />

(human monoclonal ABX-EGF heavy chain), disulfide with human<br />

monoclonal ABX-EGF light chain, dimer<br />

antineoplastic agent<br />

panitumumab immunoglobuline, anti-(récepteur du facteur de croissance épidermal<br />

humain) dimére du disulfure entre la chaîne lourde et la chaîne<br />

légère de l'anticorps monoclonal humain ABX-EGF<br />

antinéoplasique<br />

panitumumab inmunoglobulina, anti-(receptor del factor de crecimiento epidérmico<br />

humano) dímero del disulfuro entre la cadena pesada y la cadena<br />

ligera del anticuerpo monoclonal humano ABX-EGF<br />

antineoplásico<br />

C6306H9732N1672O1994S46<br />

339177-26-3<br />

pegamotecanum<br />

pegamotecan α-{2-[(2S)-1-{[(4S)-4-ethyl-3,14-dioxo-3,4,12,14-tetrahydro-<br />

1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-4-yl]oxy}-1-oxopropan-<br />

2-ylamino]-2-oxoethyl}-ω-(2-[(2S)-1-{[(4S)-4-ethyl-3,14-dioxo-<br />

3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-<br />

4-yl]oxy}-1-oxopropan-2-ylamino]-2-oxoethoxy)poly(oxyethane-<br />

1,2-diyl)<br />

antineoplastic agent<br />

pégamotécan dérivé pégylé de la camptothécine obtenu par amidification entre le<br />

(2S)-2-aminopropanoate de (4S)-4-éthyl-3,14-dioxo-3,4,12,14tétrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoléin-4-yle<br />

(L-alaninate de camptothécine) et le α-(carboxyméthyl)-<br />

ω-(carboxyméthoxy)poly(oxyéthylène)<br />

antinéoplasique

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